| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:26320899-26321047 | Rare:53; Clinvar (benign):1 | ||||
| chr4:26860606-26860798 | Common:1; Rare:62 | ||||
| chr4:30721109-30721443 | Common:3; Rare:84 | ||||
| chr4:30721978-30722166 | Common:1; Rare:61 | ||||
| chr4:36243859-36244112 | Common:2; Rare:52 | ||||
| chr4:37826544-37826724 | Common:6; Rare:64 | ||||
| chr4:38867570-38867822 | Common:2; Rare:86 | ||||
| chr4:39182202-39182562 | Common:1; Rare:81; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:39458857-39459120 | Common:3; Rare:152; Clinvar:1; Clinvar (benign):5 | ||||
| chr4:39527383-39527780 | Common:2; Rare:106 | ||||
| chr4:39527933-39527992 | Rare:12 | ||||
| chr4:39638761-39639190 | Common:1; Rare:154 | ||||
| chr4:39697997-39698188 | Common:1; Rare:74 | ||||
| chr4:40056657-40057014 | Common:4; Rare:108 | ||||
| chr4:41261712-41261922 | Rare:78; Clinvar:1 |